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Analysis of the Development Test of Visual Perception and the Motor-Free Visual Perception Test.

To identify children with learning problems and to compare test results, 28 kindergarten children were tested with the Developmental Test of Visual Perception and the Motor-free Visual Perception Test. The tests identified some children already noted by the teacher to exhibit characteristics of learning difficulty, failed to confirm the teacher's judment in others, and identified some children with previously undetected difficulties. Basic differences in the two tests are reported.

Child↗

The Visual Response Evaluation: a pilot study of an evaluation tool for assessing visual responses in low-level brain-injured patients.

The Visual Response Evaluation (VRE) was developed to meet the need for a formal and in-depth measure of visual responses in low-level brain-injured persons (Rancho Levels II and III) and to monitor and document minute changes in the recovery of these patients. Often, patients at these low functional levels exhibit little to no motoric or cognitive interaction with the environment, except that which occurs in response to sensory stimulation. Other tools have been developed to document responses to various types of stimulation; however, none contain the sensitivity to consistency and type of response that is necessary to show the small but vital progress that is characteristic of the Rancho II and II type patient. The VRE consists of 10 items separated into two general categories: (1) Observations. and (2) Response to Stimuli. The five items in the Observations section assess a patient's spontaneous responses, while the five items in the Response to Stimuli section document responses directly related to the presentation of a hierarchical order of stimuli. The VRE was administered to 10 patients with a mean age of 39.8 years at a mean time of 4.2 months post-injury. Statistical analyses of the pilot-study data show the VRE to be both internally reliable and criterion-related valid at the p less than 0.025 level of significance. The data supports further investigation in the areas of prognostic ability and implications for treatment. The VRE can be a useful tool for studying the recovery process and evaluating treatment programmes for low-level brain-injured persons.

Arousal↗

Eye movements and the integration of visual memory and visual perception.

Because visual perception has temporal extent, temporally discontinuous input must be linked in memory. Recent research has suggested that this may be accomplished by integrating the active contents of visual short-term memory (VSTM) with subsequently perceived information. In the present experiments, we explored the relationship between VSTM consolidation and maintenance and eye movements, in order to discover how attention selects the information that is to be integrated. Specifically, we addressed whether stimuli needed to be overtly attended in order to be included in the memory representation or whether covert attention was sufficient. Results demonstrated that in static displays in which the to-be-integrated information was presented in the same spatial location, VSTM consolidation proceeded independently of the eyes, since subjects made few eye movements. In dynamic displays, however, in which the to-be-integrated information was presented in different spatial locations, eye movements were directly related to task performance. We conclude that these differences are related to different encoding strategies. In the static display case, VSTM was maintained in the same spatial location as that in which it was generated. This could apparently be accomplished with covert deployments of attention. In the dynamic case, however, VSTM was generated in a location that did not overlap with one of the to-be-integrated percepts. In order to "move" the memory trace, overt shifts of attention were required.

Eye Movements↗

Prioritization in visual search: visual marking is not dependent on a mnemonic search.

Visual marking (VM) refers to our ability to completely exclude old items from search when new stimuli are presented in our visual field. We examined whether this ability reflects an attentional scan of the old items, possibly allowing observers to apply inhibition of return or maintain a memory representation of already seen locations. In four experiments, we compared performance in two search conditions. In the double-search (DS) condition, we required participants to pay attention to a first set of items by having them search for a target within the set. Subsequently, they had to search a second set while the old items remained in the field. In the VM condition, the participants expected the target only to be in the second (new) set. Selection of new items in the DS condition was relatively poor and was always worse than would be expected if only the new stimuli had been searched. In contrast, selection of the new items in the VM condition was good and was equal to what would be expected if there had been an exclusive search of the new stimuli. These results were not altered when differences in Set 1 difficulty, task switching, and response generation were controlled for. We conclude that the mechanism of VM is distinct from mnemonic and/or serial inhibition-of-return processes as involved in search, although we also discuss possible links to more global and flexible inhibition-of-return processes not necessarily related to search.

Adolescent↗

The locus of spatial attention during the temporal integration of visual memories and visual percepts.

Temporal integration is a process by which two serially presented visual stimuli are mentally integrated to form a composite representation. In the present research, we explored how spatial selective attention is used during the delay separating stimuli, in order to determine the contents of spatial working memory in this task. A two-task situation was created. On the primary task, two dot arrays were serially presented within a grid, leaving one space empty, which subjects identified. On the secondary task, instead of the second array, a discrimination probe was presented. Integration accuracy increased through delays of 1,500 msec, revealing an estimate of the time required to form an optimal memory trace for integration. Once the memory trace was formed (but not before), response time to the probe was faster if it was presented in a location previously occupied by a dot from Array 1. This indicates that during the delay separating the arrays, the subjects assigned spatial attention to the locations occupied by the first array and actively maintained the leading array in working memory. Implications for theories of visual processing and memory are discussed.

Attention↗

Why is it difficult to see in the fog? How stimulus contrast affects visual perception and visual memory.

Processing visually degraded stimuli is a common experience. We struggle to find house keys on dim front porches, to decipher slides projected in overly bright seminar rooms, and to read 10th-generation photocopies. In this research, we focus specifically on stimuli that are degraded via reduction of stimulus contrast and address two questions. First, why is it difficult to process low-contrast, as compared with high-contrast, stimuli? Second, is the effect of contrast fundamental in that its effect is independent of the stimulus being processed and the reason for processing the stimulus? We formally address and answer these questions within the context of a series of nested theories, each providing a successively stronger definition of what it means for contrast to affect perception and memory. To evaluate the theories, we carried out six experiments. Experiments 1 and 2 involved simple stimuli (randomly generated forms and digit strings), whereas Experiments 3-6 involved naturalistic pictures (faces, houses, and cityscapes). The stimuli were presented at two contrast levels and at varying exposure durations. The data from all the experiments allow the conclusion that some function of stimulus contrast combines multiplicatively with stimulus duration at a stage prior to that at which the nature of the stimulus and the reason for processing it are determined, and it is the result of this multiplicative combination that determines eventual memory performance. We describe a stronger version of this theory--the sensory response, information acquisition theory--which has at its core, the strong Bloch's-law-like assumption of a fundamental visual system response that is proportional to the product of stimulus contrast and stimulus duration. This theory was, as it has been in the past, highly successful in accounting for memory for simple stimuli shown at short (i.e., shorter than an eye fixation) durations. However, it was less successful in accounting for data from short-duration naturalistic pictures and was entirely unsuccessful in accounting for data from naturalistic pictures shown at longer durations. We discuss (1) processing differences between short- and long-duration stimuli, (2) processing differences between simple stimuli, such as digits, and complex stimuli, such as pictures, (3) processing differences between biluminant stimuli (such as line drawings with only two luminance levels) and multiluminant stimuli (such as grayscale pictures with multiple luminance levels), and (4) Bloch's law and a proposed generalization of the concept of metamers.

Fixation, Ocular↗

Contribution of somatosensory information to perception of the visual vertical with body tilt and rotating visual field.

This study was designed to explore the role of somatosensory information from the trunk in the perception of the visual vertical. Twelve normal subjects and 1 subject with no somatosensory function below the neck attempted to set a line to the true vertical in the sitting and lying positions, first with a static visual background and then with rotation of the background about the line of sight. The absence of somatosensory information did not affect accuracy when the subjects were in the upright position. When lying horizontally, all control subjects experienced a substantial perceived tilt of the vertical in the direction of body tilt (the A effect), but, in contrast, the subject lacking somatosensory function exhibited a small but consistent apparent tilt of the vertical in the opposite direction (the E effect). This finding is discussed in relation to two competing hypotheses regarding the mechanisms subserving apparent displacement of the subjective vertical in tilted subjects.

Adolescent↗

[Responses of squirrel visual cortex neurons to patterned visual stimuli].

The responses of visual cortical neurons to patterned visual stimuli were studied in squirrel Sciurus vulgaris. The direction selective, orientation-selective and non-selective neurons were observed. Most direction-selective and non-selective neurons were sensitive to high speeds of stimulus movement--hundreds deg/s. The direction-selective neurons exhibited their selectivity at such high speeds in spite of the short time of the stimulus movement through the receptive field. Orientation-selective neurons (with simple or complex receptive fields) were sensitive to lower speeds of the stimulus movement (tens deg/s). Some mechanisms of the properties described are discussed.

Animals↗

[Visual field change and risk factors for progression of visual field damage in low tension glaucoma].

The authors carried out a prospective study in an attempt to determine the possible effect of intraocular pressure (IOP) and some clinical factors on the clinical course of low tension glaucoma (LTG). During the study period all the patients were followed without any antiglaucoma medication. The enrollment criteria for the study were reproducible, mild to moderate field loss as defined as a mean defect (MD) of greater than 2 dB and less than 10 dB or corrected loss variance (CLV) of greater than 7 dB revealed by the Octopus 201, G1 program. Forty-two consecutive patients (56 eyes) who fulfilled this criteria were enrolled. Baseline and follow-up examinations included applanation tonometry, perimetry with G1 program, blood pressure and pulse rate. When the MD increased by 4 dB or more on two consecutive perimetry examinations, the field defect was judged as "progressed". During the follow-up period (6-51 months, 25.1 +/- 12.5 months), the field defect progressed in 14 eyes of 12 patients. The life-table analysis (Kaplan-Meier) revealed that the rate of nonprogression of visual field defects was 55.5% at 48 months. The rate of nonprogression was significantly lower in 16 eyes with a mean IOP equal to or higher than 15 mmHg as opposed to 40 eyes with that lower than 15 mmHg (34.3% and 67.2% respectively, p less than 0.05). The results seem to indicate that IOP is likely to be responsible for the aggravation of visual fields in LTG. Canonical discriminant analysis revealed that the discriminant function containing four variables gives the best separation between the "progressed" and "nonprogressed" group (discriminant efficacy: 83.9%).

Adult↗

[Evaluation of the visual evoked potentials in relation to the type of visual stimulation].

A classification of visual evoked potentials (VEP) in children and adults in response to various types of vision stimulation has been developed. Four major signs underlie this classification: (1) stimulation time frequency; (2) stimulation type; (3) mode of producing the visuals stimulus; (4) mono- or binocular presentation of the stimulus. One more sign can be added to classification: significant parameters of stimulation. Basing on this classification, the author describes the major VEP modalities and gives recommendations on the practical employment of these modalities.

Adult↗

Visual cortex development in the ferret. I. Genesis and migration of visual cortical neurons.

The production of ferret visual cortical neurons was studied using 3H-thymidine autoradiography. The genesis of cortical neurons begins on or slightly before embryonic day 20 (E20) of the 41 d gestational period, continues postnatally until 2 weeks after birth (P14), and follows an inside-out radial gradient with neurons for the deeper cortical layers being generated before those for the superficial layers. Layer I neurons are generated both early (E20-E30) and late (P1-P14) in the period of cortical neurogenesis and, thus, provide at least a partial exception to the inside-out gradient of cortical neurogenesis. Tangential gradients of cortical neurogenesis extend across areas 17 and 18 in both the anterior-to-posterior and lateral-to-medial directions. Neither of these gradients bears a meaningful relationship to the cortical representation of the visual field. Most infragranular and granular layer neurons are generated prenatally, while most supragranular layer neurons are produced postnatally. Neurons destined for a given layer are produced over a period of several days, and the neurons generated on any given day contribute to the formation of 2 or more cortical layers. In general, prenatally generated neurons complete their migration in 1 week or less, while most postnatally generated neurons require approximately 2 weeks to complete their migration.

Animals↗

Disconnection of the amygdala from visual association cortex impairs visual reward-association learning in monkeys.

Cynomolgus monkeys (Macaca fascicularis) were trained in a task that assessed their ability to associate visual stimuli with food reward. Acquisition of stimulus-reward associations was measured under 2 conditions, a 2-stimuli acquisition condition and a 1-stimulus acquisition condition. On each trial in the 2-stimuli condition, the positive (correct) and negative (incorrect) stimuli were presented side by side and the animal chose one by touching it; if the choice was correct, a food reward was dispensed. On each trial in the 1-stimulus condition, either the positive or the negative stimulus was presented alone; if the stimulus was the positive, it was followed by reward delivery, regardless of the animal's response to it, and if it was the negative, it was not followed by reward delivery. Thus, reward delivery was contingent upon the animal's response to the stimuli in the 2-stimuli condition but not in the 1-stimulus condition. The effect of acquisition trials under these 2 conditions was measured, in both conditions, by the animal's subsequent choice when presented with the 2 stimuli side by side. Following preoperative training in this task, the animals were first subjected to unilateral ablation of the inferotemporal cortex. This operation had little effect on the animals' learning ability. Then, the amygdala was ablated in the hemisphere contralateral to that in which the unilateral inferotemporal ablation had been carried out. This combination of crossed unilateral lesions of the amygdala and of the inferotemporal cortex, which disconnects the amygdala from the output of visual association cortex, produced a profound impairment in stimulus-reward-associative learning.(ABSTRACT TRUNCATED AT 250 WORDS)

Acoustic Stimulation↗

The application of a comprehensive visual screening programme to children aged 3-5 years. Can a modified procedure be devised for visual screening by ancillary staff?

Current commercially available tests to examine visual performance in children are discussed and adapted for a visual screening programme applied to 249 children aged 3-5 years at school or playgroup premises. Correlation of refractive and ocular muscle findings with the remaining tests is evaluated. A simplified screening procedure is thereby recommended which may be undertaken by ancillary staff, without any need for sophisticated equipment. This would enable identification, for further examination, of most children whose refraction and eye coordination are outside normal limits.

Age Factors↗

Computer automated visual acuity testing for visual screening.

A computer program was designed for automated visual acuity testing, the aim of which was to evaluate the effectiveness of such systems in a busy out-patient department. The time required for explanation and performing the automated test was compared with that taken by nurses measuring visual acuities in the conventional manner using a Snellen's chart. The correlation of the results of the computer system and the manual measurements was tested.

Adolescent↗

[Effect of early visual deprivation on glutamate decarboxylase activity in the visual analyzer of the brain].

Early vision deprivation decreased in dogs (45-days age) the activity of glutamate decarboxylase in all the structures of brain visual analyzer studied as well as decreased the enzyme activation by exogenous pyridoxal-5-phosphate. With areing (in 90-days old dogs) the deprivation proved to be less effective in relation to decrease in the glutamate decarboxylase activity in external geniculate body but caused the same affect in the visual zone of brain cortex and in anterior mesencephalon. The deprivation exhibited similar effect on formation of asparaginic acid.

Age Factors↗

[Acetylcholinesterase activity in visual cortex structures during early visual deprivation].

By means of quantitative histochemical methods it has been shown that an early photic deprivation (animals kept in a dark chamber for two months after their birth) leads to a decrease in the activity level of acetylcholinesterase (AChE) in the visual area of the cerebral cortex. With the recovery of the visual function (animals kept in normal photic conditions for two weeks) the AChE activity becomes markedly normalized. The obtained data allow to suggest that the decrease in AChE activity due to deprivation is functionally determined.

Acetylcholine↗

[Postnatal development of functional properties of the visual cortical cells of area 18 in kittens raised with or without visual experience].

866 units were recorded extracellularly in area 18 of anaesthetized and paralysed kittens from 13 to 66 days of age. The development of their receptive field properties was studied in normally (EN) and dark-reared (EO) kittens. In addition to orientation selective (S) and non-selective (NS) cells, we found a number of non-selective units whose receptive field was surrounded by a peripheral zone (NSp) where stationary stimuli were effective. In EN kittens, the orientation selectivity developed with age and concomitantly, NS and NSp cells disappeared. Ocular dominance distribution was also gradually modified from a contralateral monocular dominance at 13 days of age to an adult-like binocularity at 58 days. In EO kittens, the early orientation selectivity began to decrease at the 5th week. From then on, the process of despecification started and progressed until nearly all cells were NS. Absence of visual experience also delayed the development of mature binocularity. In 6 week old EO kittens, a 6 hrs. visual exposure induced a fast but uncomplete specification with decrease of both NS and NSp cells and a slight modification of the ocular dominance distribution. The comparison of these results with those obtained in area 17 shows that functional properties vary more slowly in area 18 than in area 17.

Animals↗

[Visual evoked potentials in reversal and motion-onset stimulation of visual fields in patients with retrobulbar neuritis].

In 21 patients with unilateral retrobulbar neuritis the pattern reversal evoked potentials and motion-onset visual potentials were investigated with the aim to find out whether there is some difference in affection of pattern detecting (parvocellular) and motion detecting (magnocellular) visual pathways in this disease. The pattern reversal potentials were found to be abnormal in all 21 patients: they showed either significantly prolonged latencies and reduced amplitudes of the main positive P100 peak or no clear response (in one patient) upon the stimulation of the eye with neuritis. In contrast, the main negative peak of the motion-onset potentials was significantly delayed only in 15 patients and its amplitude was distinctly reduced only in 3 patients. The results indicate that in retrobulbar neuritis the pattern detecting nerve fibres from the central part of the retina (tested by reversal potentials) are affected earlier and to a greater extent than the more peripherally distributed motion detecting fibres (tested by motion-onset potentials).

Adult↗